Veszeli N

No ORCID on file · 1 paper in corpus
2019
Orphanet journal of rare diseases ·doi:10.1186/s13023-019-0995-7

Background and aimsHereditary angioedema with C1-inhibitor deficiency (C1-INH-HAE) is characterized by localized, non-pitting, and transient swelling of submucosal or subcutaneous region. Human fetuin-A is a multifunctional glycoprotein tha…